New Mutation Associated with Polycystic Kidney Disease Type I: A Case Report.

INTRODUCTION

Autosomal dominant polycystic kidney disease (ADPKD) is one of the most prevalent heritable disorders, characterized by the progressive development of kidney cysts leading to renal failure. It is primarily caused by mutations in the and genes, which account for approximately 85% and 15% of cases, respectively. This case report describes a previously unreported mutation in the gene, identified in a family involving an aunt and her niece with ADPKD.

CASE PRESENTATION

The index case, a 56-year-old female with chronic kidney disease stage 3b secondary to ADPKD and hypertension, exhibited a strong family history of polycystic kidney disease (PKD). Initial genetic evaluations did not identify any recognized pathogenic mutations, leading to a more detailed investigation which revealed a novel mutation in the gene. This mutation was also found in her niece, who presented with early-onset disease.

CONCLUSIONS

The identification of a heterozygous six-nucleotide deletion, c.2084_2089del, resulting in the in-frame deletion of two amino acids, p.Pro695_Ala696del, in the gene, has been linked with ADPKD in these patients. This report emphasizes the need for continuous updates to genetic data for a deeper understanding of the diagnosis and prognosis of ADPKD that could potentially aid in targeted therapy.